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} | } | ||
+ | h2 span { | ||
+ | color: white; | ||
+ | font: 100px/100px Helvetica, Sans-Serif; | ||
+ | letter-spacing: 10px; | ||
+ | background: rgb(0, 0, 0); /* fallback color */ | ||
+ | background: rgba(0, 0, 0, 0.7); | ||
+ | padding: 10px; | ||
+ | |||
+ | h2 { | ||
+ | position: absolute; | ||
+ | top: 350px; | ||
+ | left: 0; | ||
+ | width: 100%; | ||
+ | } | ||
+ | } | ||
</style> | </style> | ||
Revision as of 14:24, 27 October 2017
RESULTS
OBJECTIVE: CREATE pgRNA
OBJECTIVE: CREATE pREPORTER
OBJECTIVE: PROMOTER LIBRARY
OBJECTIVE: RANDOM LIGATIONS
OBJECTIVE: FREEZE DRYING
OBJECTIVE: CRISPRi & gRNA EFFICIENCY
This picture shows our gRNAs working visually, but the graphs show the results of RFP detection using a microplate reader on cultures containing each of the dCas9 plasmids with one promoter-RFP-terminator brick, with its corresponding gRNA plasmid, or with a non-targeting gRNA plasmid.